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The protein encoded by TCF12 is a member of the basic helix-loop-helix (bHLH) E-protein family that recognizes the consensus binding site (E-box) CANNTG. Zusätzlich bieten wir Ihnen TCF12 Proteine (7) und viele weitere Produktgruppen zu diesem Protein an.
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Cow (Bovine) Polyclonal TCF12 Primary Antibody für WB - ABIN2780487
Lazrek, Goffard, Schanen, Karquel, Bocket, Lion, Devaux, Hedouin, Gosset, Hober: Detection of hepatitis C virus antibodies and RNA among medicolegal autopsy cases in Northern France. in Diagnostic microbiology and infectious disease 2006
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Chicken Polyclonal TCF12 Primary Antibody für WB - ABIN2774659
Wissmüller, Kosian, Wolf, Finzsch, Wegner: The high-mobility-group domain of Sox proteins interacts with DNA-binding domains of many transcription factors. in Nucleic acids research 2006
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Human Polyclonal TCF12 Primary Antibody für EIA, WB - ABIN783743
Murre, McCaw, Vaessin, Caudy, Jan, Jan, Cabrera, Buskin, Hauschka, Lassar: Interactions between heterologous helix-loop-helix proteins generate complexes that bind specifically to a common DNA sequence. in Cell 1989
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Human Polyclonal TCF12 Primary Antibody für EIA, WB - ABIN955126
Schotte, Dontje, Nagasawa, Yasuda, Bakker, Spits, Blom: Synergy between IL-15 and Id2 promotes the expansion of human NK progenitor cells, which can be counteracted by the E protein HEB required to drive T cell development. in Journal of immunology (Baltimore, Md. : 1950) 2010
HEB may be involved in GBM cell proliferation, as HEB silencing reduced proliferation in cells cultured as monolayers or neurospheres. Furthermore, the results suggested a potential role for HEB in the maintenance of GBM stem cells, as HEB silencing affected the differentiation capacity of cells.
Two novel translocations leading to the inactivation of RUNX1 (zeige RUNX1 Antikörper) and its partners SIN3A (zeige SIN3A Antikörper) and TCF12 in myeloid leukemia (zeige BCL11A Antikörper).
Studies suggest that transcription factor 12 (TCF12) should be included in level 2 genetic testing.
show that these mutations compromise TCF12 transcriptional activity and are associated with a more aggressive tumour type
several familial cases of coronal synostosis associated with mutations in TCF12
In t(8;21) leukemia cells, the two E proteins, HEB and E2A (zeige TCF3 Antikörper), function as components of the stable AML1 (zeige RUNX1 Antikörper)-ETO (zeige RUNX1T1 Antikörper)-containing transcription factor complex (AETFC). The AETFC components cooperatively regulate gene expression and contribute to leukemogenesis.
haploinsufficiency of TCF12 causes coronal synostosis in humans and that severe bilateral coronal synostosis occ (zeige TWIST1 Antikörper)urs in mice with 50% of the wild-type dosage of both the T (zeige TWIST1 Antikörper)cf12 and Twist1 genes highlights the key role of TCF12 acting with TWIST1.
the CD91 (zeige LRP1 Antikörper)/IKK (zeige CHUK Antikörper)/NF-kappaB (zeige NFKB1 Antikörper) signaling cascade is involved in secreted HSP90alpha (zeige HSP90AA2 Antikörper)-induced TCF12 expression, leading to E-cadherin (zeige CDH1 Antikörper) down-regulation and enhanced CRC (zeige CALR Antikörper) cell migration/invasion
TCF12 functioned as a transcriptional repressor of E-cadherin (zeige CDH1 Antikörper) and its overexpression was significantly correlated with the occurrence of CRC (zeige CALR Antikörper) metastasis.
HEB and E2A (zeige TCF3 Antikörper)-bind the SCA motif at regions overlapping SMAD2 (zeige SMAD2 Antikörper)/3 and FOXH1 (zeige FOXH1 Antikörper)
HEB (zeige FREM1 Antikörper) is a fundamental link between Nodal signalling, the derepression of a specific class of poised promoters during differentiation, and lineage specification in mouse embryonic stem cells
severe bilateral coronal synostosis occurs in mice with 50% of the wild-type dosage of both the Tcf12 and Twist1 (zeige TWIST1 Antikörper) genes highlights the key role of TCF12 acting with TWIST1 (zeige TWIST1 Antikörper) in the normal development of the coronal sutures
Deficiency in the E proteins, E2A (zeige TCF3 Antikörper) and HEB (zeige FREM1 Antikörper), led to increased frequency of terminally differentiated effector KLRG1 (zeige KLRG1 Antikörper)(hi) CD8 (zeige CD8A Antikörper)(+) T cells in mice during infection, and decreased generation of longer-lived memory-precursor cells during the immune response.
Deletion of HEB (zeige FREM1 Antikörper) and E2A (zeige TCF3 Antikörper) in DP thymocytes specifically blocked the development of CD4 (zeige CD4 Antikörper)(+) lineage T cells. Furthermore, deletion of the E protein inhibitors Id2 and Id3 (zeige ID3 Antikörper) allowed CD4 (zeige CD4 Antikörper)(+) T cell development but blocked CD8 (zeige CD8A Antikörper)(+) lineage development.
the earliest event in B-cell specification involves the induction of FOXO1 (zeige FOXO1 Antikörper) expression and requires the combined activities of E2A (zeige TCF3 Antikörper) and HEB (zeige FREM1 Antikörper)
These results showed a new set of interactions between HEB (zeige FREM1 Antikörper), Notch1 (zeige NOTCH1 Antikörper), and GATA3 (zeige GATA3 Antikörper) that regulate the T-cell fate choice in developing thymocytes.
Developmental progression of fetal HEB (zeige FREM1 Antikörper)(-/-) precursors to the pre-T-cell stage is restored by HEBAlt.
HEB (zeige FREM1 Antikörper) is a specific and essential factor in T-cell development and in the generation of the iNKT cell lineage.
the dosage of HEB (zeige FREM1 Antikörper) determines pT alpha (zeige PTCRA Antikörper) gene expression in immature T cells
the Tcf12 gene may be involved in the control of proliferating neural stem cells and progenitor cells
The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH) E-protein family that recognizes the consensus binding site (E-box) CANNTG. This encoded protein is expressed in many tissues, among them skeletal muscle, thymus, B- and T-cells, and may participate in regulating lineage-specific gene expression through the formation of heterodimers with other bHLH E-proteins. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.
transcription factor 12
, transcription factor 12 (HTF4, helix-loop-helix transcription factors 4)
, DNA-binding protein HTF4
, E-box-binding protein
, class B basic helix-loop-helix protein 20
, helix-loop-helix transcription factor 4
, transcription factor HTF-4
, class A helix-loop-helix transcription factor ME1
, SCBP alpha
, salivary-specific cAMP response element-binding protein alpha
, basic helix-loop-helix protein
, class A helix-loop-helix transcription factor GE1